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Plasmid DNA contaminant in molecular reagents

Background noise in metagenomic studies is often of high importance and its removal requires extensive post-analytic, bioinformatics filtering. This is relevant as significant signals may be lost due to a low signal-to-noise ratio. The presence of plasmid residues, that are frequently present in rea...

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Autores principales: Wally, N., Schneider, M., Thannesberger, J., Kastner, M. T., Bakonyi, T., Indik, S., Rattei, T., Bedarf, J., Hildebrand, F., Law, J., Jovel, J., Steininger, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367390/
https://www.ncbi.nlm.nih.gov/pubmed/30733546
http://dx.doi.org/10.1038/s41598-019-38733-1
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author Wally, N.
Schneider, M.
Thannesberger, J.
Kastner, M. T.
Bakonyi, T.
Indik, S.
Rattei, T.
Bedarf, J.
Hildebrand, F.
Law, J.
Jovel, J.
Steininger, C.
author_facet Wally, N.
Schneider, M.
Thannesberger, J.
Kastner, M. T.
Bakonyi, T.
Indik, S.
Rattei, T.
Bedarf, J.
Hildebrand, F.
Law, J.
Jovel, J.
Steininger, C.
author_sort Wally, N.
collection PubMed
description Background noise in metagenomic studies is often of high importance and its removal requires extensive post-analytic, bioinformatics filtering. This is relevant as significant signals may be lost due to a low signal-to-noise ratio. The presence of plasmid residues, that are frequently present in reagents as contaminants, has not been investigated so far, but may pose a substantial bias. Here we show that plasmid sequences from different sources are omnipresent in molecular biology reagents. Using a metagenomic approach, we identified the presence of the (pol) of equine infectious anemia virus in human samples and traced it back to the expression plasmid used for generation of a commercial reverse transcriptase. We found fragments of multiple other expression plasmids in human samples as well as commercial polymerase preparations. Plasmid contamination sources included production chain of molecular biology reagents as well as contamination of reagents from environment or human handling of samples and reagents. Retrospective analyses of published metagenomic studies revealed an inaccurate signal-to-noise differentiation. Hence, the plasmid sequences that seem to be omnipresent in molecular biology reagents may misguide conclusions derived from genomic/metagenomics datasets and thus also clinical interpretations. Critical appraisal of metagenomic data sets for the possibility of plasmid background noise is required to identify reliable and significant signals.
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spelling pubmed-63673902019-02-11 Plasmid DNA contaminant in molecular reagents Wally, N. Schneider, M. Thannesberger, J. Kastner, M. T. Bakonyi, T. Indik, S. Rattei, T. Bedarf, J. Hildebrand, F. Law, J. Jovel, J. Steininger, C. Sci Rep Article Background noise in metagenomic studies is often of high importance and its removal requires extensive post-analytic, bioinformatics filtering. This is relevant as significant signals may be lost due to a low signal-to-noise ratio. The presence of plasmid residues, that are frequently present in reagents as contaminants, has not been investigated so far, but may pose a substantial bias. Here we show that plasmid sequences from different sources are omnipresent in molecular biology reagents. Using a metagenomic approach, we identified the presence of the (pol) of equine infectious anemia virus in human samples and traced it back to the expression plasmid used for generation of a commercial reverse transcriptase. We found fragments of multiple other expression plasmids in human samples as well as commercial polymerase preparations. Plasmid contamination sources included production chain of molecular biology reagents as well as contamination of reagents from environment or human handling of samples and reagents. Retrospective analyses of published metagenomic studies revealed an inaccurate signal-to-noise differentiation. Hence, the plasmid sequences that seem to be omnipresent in molecular biology reagents may misguide conclusions derived from genomic/metagenomics datasets and thus also clinical interpretations. Critical appraisal of metagenomic data sets for the possibility of plasmid background noise is required to identify reliable and significant signals. Nature Publishing Group UK 2019-02-07 /pmc/articles/PMC6367390/ /pubmed/30733546 http://dx.doi.org/10.1038/s41598-019-38733-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wally, N.
Schneider, M.
Thannesberger, J.
Kastner, M. T.
Bakonyi, T.
Indik, S.
Rattei, T.
Bedarf, J.
Hildebrand, F.
Law, J.
Jovel, J.
Steininger, C.
Plasmid DNA contaminant in molecular reagents
title Plasmid DNA contaminant in molecular reagents
title_full Plasmid DNA contaminant in molecular reagents
title_fullStr Plasmid DNA contaminant in molecular reagents
title_full_unstemmed Plasmid DNA contaminant in molecular reagents
title_short Plasmid DNA contaminant in molecular reagents
title_sort plasmid dna contaminant in molecular reagents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367390/
https://www.ncbi.nlm.nih.gov/pubmed/30733546
http://dx.doi.org/10.1038/s41598-019-38733-1
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